HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18184366, compound → HCID 18184387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18184366 | HCID 18184366 | — |
| Reactant | HCID 69704031 | HCID 69704031 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 18184387 | HCID 18184387 | — |
Reaction Steps
Scheme 2 can be illustrated with reference to the preparation of 4-oxo-3H-oxazolo[5,4-g]quinazoline. In this process, 5-hydroxy-2,4-dinitrobenzamide (compound of formula VIII in which Y1 is amino, Y2 is O, Y4 is hydroxy and Y5 is nitro) is hydrogenated over 5% palladium over carbon at about 60 psi for about 3 hours to give 2,4-diamino-5-hydroxybenzamide. To this product is added formic acid and the mixture is heated to reflux for about 48 hours to provide 4-oxo-3H-oxazolo[5,4-g]quinazoline. In this process, steps 1 and 2 of Scheme 2 are performed as a single step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335344B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-f7ceae22eb8049af87fe7113330ab547 |
| Source note | uspto-grants-2002_01 |